FDA.reportPublic FDA data

RICHENNA PHARM HAND SANI FLUID gel

Manufacturer
SEWHA P&C INC.
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:52

Label at a glance#

ProductRICHENNA PHARM HAND SANI FLUID gel
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Put nough produt in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

ANTISEPTIC

Use

INDICATIONS & USAGE SECTION

  • For Hand Sanitizing to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put nough produt in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Menthol, Isopropyl Myristate, C11-15 Pareth-12, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30Alkyl Acrylate Crosspolymer, Triethanolamine, Betaine, Artemisia Princeps Extract, Angelica Gigas Root Extract, Ginkgo Biloba Leaf Extract, Parfum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50629-00150629-001-01, 50629-001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
C11-15 PARETH-12DB048RC6PYIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
BETAINE3SCV180C9WIACT
ARTEMISIA PRINCEPS LEAFSY077EW02GIACT
ANGELICA GIGAS ROOT32766B2FHXIACT
GINKGO19FUJ2C58TIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ecaf87b9-66e5-1e1e-e053-2995a90a24cacc014fa3-699d-43ab-bbd2-1fce27f3f5352022-11-04WarningsExact identifier
spl set id: cc014fa3-699d-43ab-bbd2-1fce27f3f535

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.